Variant report

Variant	rs4263291
Chromosome Location	chr3:115825220-115825221
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11425708	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11918080	0.98[ASN][1000 genomes]
rs12695321	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13100914	0.90[ASN][1000 genomes]
rs13318106	0.81[EUR][1000 genomes]
rs1344131	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17630430	0.80[ASN][1000 genomes]
rs17697994	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1920379	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2091669	0.98[ASN][1000 genomes]
rs2222827	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2864066	0.92[ASN][1000 genomes]
rs2864067	0.92[ASN][1000 genomes]
rs28735793	0.82[ASN][1000 genomes]
rs33956431	0.88[ASN][1000 genomes]
rs34523792	0.80[ASN][1000 genomes]
rs34844901	0.88[ASN][1000 genomes]
rs34930794	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35242629	0.88[ASN][1000 genomes]
rs35619123	0.88[ASN][1000 genomes]
rs35780065	0.88[ASN][1000 genomes]
rs35914238	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4831227	0.88[ASN][1000 genomes]
rs4831228	0.98[ASN][1000 genomes]
rs4831229	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4831230	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5004406	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56121547	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62269168	1.00[ASN][1000 genomes]
rs62269170	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66490447	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6765355	0.98[ASN][1000 genomes]
rs6772113	0.98[ASN][1000 genomes]
rs73139202	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7632265	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7637650	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9289042	0.89[ASN][1000 genomes]
rs9813038	0.89[ASN][1000 genomes]
rs9816425	0.98[ASN][1000 genomes]
rs9821865	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9822568	0.98[ASN][1000 genomes]
rs9827733	0.81[EUR][1000 genomes]
rs9836963	0.88[ASN][1000 genomes]
rs9837276	0.88[ASN][1000 genomes]
rs9839078	0.98[ASN][1000 genomes]
rs9851643	0.80[ASN][1000 genomes]
rs9854345	0.88[ASN][1000 genomes]
rs9854711	0.98[ASN][1000 genomes]
rs9855097	0.98[ASN][1000 genomes]
rs9857520	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9866484	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9866658	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9873576	0.94[ASN][1000 genomes]
rs9877662	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9985471	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012260	chr3:115680931-115935968	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2756413	chr3:115721898-115908480	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv2751975	chr3:115766285-115902901	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv2755046	chr3:115818840-115942952	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv591345	chr3:115819376-115902901	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115780400-115830000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:115822600-115827400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:115824000-115827400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr3:115824000-115830000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:115824200-115830000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr3:115824200-115837200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:115824400-115826000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr3:115825200-115826200	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr3:115825200-115827400	Active TSS	HUES6 Cell Line	embryonic stem cell

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